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Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Copper (metabolism) »
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Copper (deficiency) < Copper (metabolism) < Copper (pharmacology)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 6.
Ident.Authors (with country if any)Title
000B13 (2003) John M. Walshe [Royaume-Uni]The story of penicillamine: a difficult birth.
001394 (2005) John M. Walshe [Royaume-Uni]Diagnostic significance of reduced serum caeruloplasmin concentration in neurological disease.
001482 (2006) Graznya Gromadzka [Pologne] ; Harmut H J. Schmidt ; Janine Genschel ; Bettina Bochow ; M. Rodo ; Beatek Tarnacka ; Thomas Litwin ; Grzegorz Chabik ; Anna Członkowskap.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.
001731 (2006) Antje Mueller [Allemagne] ; Ulrike Reuner ; Basile Landis ; Hagen Kitzler ; Heinz Reichmann ; Thomas HummelExtrapyramidal symptoms in Wilson's disease are associated with olfactory dysfunction.
002714 (2009) Giovanni Antonio Cocco ; Georgios Loudianos ; Giovanni Mario Pes ; Francesco Tolu ; Maria Barbara Lepori ; Marianna Barrocu ; Gian Pietro Sechi"Acquired" hepatocerebral degeneration in a patient heterozygote carrier for a novel mutation in ATP7B gene.
003991 (2013) Yves Denoyer ; France Woimant ; Muriel Bost ; Gilles Edan ; Sophie DrapierNeurological Wilson's disease lethal for the son, asymptomatic in the father.

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